Details for GNRH1:c.60_61insC, p.Cys21LeufsTer23

CHROMOSOME 8
GENOMIC COORDINATES
hg19hg38
2528079825423282
VARIANT EFFECT None
ANNOTATION FLAG None
GENE GNRH1
REFERENCE ALLELE A
ALTERNATE ALLELE AG
TRANSCRIPT N.A.
CDNA CHANGE c.60_61insC
PROTEIN CHANGE p.Cys21LeufsTer23
ALLELE FREQUENCY
1KGP
GlobalAFRAMREASEURSAS
NoneNoneNoneNoneNoneNone

Gnomad
GlobalAFRAMRASJEASFINNFEOTHSAS
NoneNoneNoneNoneNoneNoneNoneNoneNone

ESP
AAEA
NoneNone
PREDICTORS
siftpp2 hvarcaddmutationtaster
NoneNone2.22606Disease causing
DBSNP ID NA
1 combination linked to GNRH1:c.60_61insC, p.Cys21LeufsTer23 OLI1168
1 disease linked to GNRH1:c.60_61insC, p.Cys21LeufsTer23 Kallmann syndrome
Found any issues with the data on this page? Report this entry.